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Stress velocity, influence

Mixing layers, which occur in many engineering applications, are shear layers between fluid streams of different velocities and are characterised by transfer of mass, momentum and energy due to vortex formation. For mixing layers with density stratification, buoyancy forces are important besides shear stress and influence considerably the intensity of mixing. Stratification has been recognised to be of importance in heat exchange between sodium streams of different temperature in the upper plenum of FBRs under decay-heat-removal conditions. [Pg.228]

The interfacial shear stress is influenced by both the interface velocity and the mixture side velocity. Moreover, the entrainment from a liquid film is associated with the onset of disturbance waves at the interface and, in general, depends on both the vapor and the liquid flow rates. In fully turbulent flow, above a film Reynolds number of 3000 the condition for the onset of entrainment depend mainly upon the vapor velocity [5]. For this reason, the fothers in Equation (2) is correlated as. [Pg.118]

Consistent with this model, foams exhibit plug flow when forced through a channel or pipe. In the center of the channel the foam flows as a soHd plug, with a constant velocity. AH the shear flow occurs near the waHs, where the yield stress has been exceeded and the foam behaves like a viscous Hquid. At the waH, foams can exhibit waH sHp such that bubbles adjacent to the waH have nonzero velocity. The amount of waH sHp present has a significant influence on the overaH flow rate obtained for a given pressure gradient. [Pg.430]

If fluid shear stresses are likely to be involved in obtaining a process result, then one must qualitatively look at the scale at which the shear stresses influence the resiilt. If the particles, bubbles, droplets, or fluid clumps are on the order of 1000 [Lm or larger, the variables are macro scale and average velocities at a point are the predominant variable. [Pg.1625]

Beyond the simple resistance of a material of construction to dissolution in a given chemical, many other properties enter into consideration when makiug an appropriate or optimum MOC selection for a given environmental exposure. These factors include the influence of velocity, impurities or contaminants, pH, stress, crevices, bimetallic couples, levels of nuclear, UV, or IB radiation, microorganisms, temperature heat flux, stray currents, properties associatea with original production of the material and its subsequent fabrication as an item of equipment, as well as other physical ana mechanical properties of the MOC, the Proverbial Siebert Changes in the Phase of the Moon, and so forth. [Pg.2442]

Electrochemical corrosion is understood to include all corrosion processes that can be influenced electrically. This is the case for all the types of corrosion described in this handbook and means that data on corrosion velocities (e.g., removal rate, penetration rate in pitting corrosion, or rate of pit formation, time to failure of stressed specimens in stress corrosion) are dependent on the potential U [5]. Potential can be altered by chemical action (influence of a redox system) or by electrical factors (electric currents), thereby reducing or enhancing the corrosion. Thus exact knowledge of the dependence of corrosion on potential is the basic hypothesis for the concept of electrochemical corrosion protection processes. [Pg.29]

Cross-flow filtration systems utilize high liquid axial velocities to generate shear at the liquid-membrane interface. Shear is necessary to maintain acceptable permeate fluxes, especially with concentrated catalyst slurries. The degree of catalyst deposition on the filter membrane or membrane fouling is a function of the shear stress at the surface and particle convection with the permeate flow.16 Membrane surface fouling also depends on many application-specific variables, such as particle size in the retentate, viscosity of the permeate, axial velocity, and the transmembrane pressure. All of these variables can influence the degree of deposition of particles within the filter membrane, and thus decrease the effective pore size of the membrane. [Pg.285]

The spreading behavior of droplets on a non-flat surface is not only dependent on inertia and viscous effects, but also significantly influenced by an additional normal stress introduced by the curved surface. This stress leads to the acceleration-deceleration effect, or the hindering effect depending on the dimensionless roughness spacing, and causes the breakup and ejection of liquid. Increasing impact velocity, droplet diameter, liquid density, and/or... [Pg.201]

The notion of fluid strains and stresses and how they relate to the velocity field is one of the fundamental underpinnings of the fluid equations of motion—the Navier-Stokes equations. While there is some overlap with solid mechanics, the fact that fluids deform continuously under even the smallest stress also leads to some fundamental differences. Unlike solid mechanics, where strain (displacement per unit length) is a fundamental concept, strain itself makes little practical sense in fluid mechanics. This is because fluids can strain indefinitely under the smallest of stresses—they do not come to a finite-strain equilibrium under the influence of a particular stress. However, there can be an equilibrium relationship between stress and strain rate. Therefore, in fluid mechanics, it is appropriate to use the concept of strain rate rather than strain. It is the relationship between stress and strain rate that serves as the backbone principle in viscous fluid mechanics. [Pg.28]

Figure 6.2. Relations between shear stress, deformation rate, and viscosity of several classes of fluids, (a) Distribution of velocities of a fluid between two layers of areas A which are moving relatively to each other at a distance x wider influence of a force F. In the simplest case, F/A = fi(du/dx) with ju constant, (b) Linear plot of shear stress against deformation, (c) Logarithmic plot of shear stress against deformation rate, (d) Viscosity as a function of shear stress, (e) Time-dependent viscosity behavior of a rheopectic fluid (thixotropic behavior is shown by the dashed line). (1) Hysteresis loops of time-dependent fluids (arrows show the chronology of imposed shear stress). Figure 6.2. Relations between shear stress, deformation rate, and viscosity of several classes of fluids, (a) Distribution of velocities of a fluid between two layers of areas A which are moving relatively to each other at a distance x wider influence of a force F. In the simplest case, F/A = fi(du/dx) with ju constant, (b) Linear plot of shear stress against deformation, (c) Logarithmic plot of shear stress against deformation rate, (d) Viscosity as a function of shear stress, (e) Time-dependent viscosity behavior of a rheopectic fluid (thixotropic behavior is shown by the dashed line). (1) Hysteresis loops of time-dependent fluids (arrows show the chronology of imposed shear stress).
Fig. 3.4 The (a) shear stress, (b) shear rate, and (c) velocity profiles of a Newtonian and a shearthinning fluid flowing in a capillary of dimensions R is under the influence of the same AP, that is, r(r). Fig. 3.4 The (a) shear stress, (b) shear rate, and (c) velocity profiles of a Newtonian and a shearthinning fluid flowing in a capillary of dimensions R is under the influence of the same AP, that is, r(r).

See other pages where Stress velocity, influence is mentioned: [Pg.368]    [Pg.1079]    [Pg.79]    [Pg.93]    [Pg.151]    [Pg.206]    [Pg.90]    [Pg.91]    [Pg.327]    [Pg.187]    [Pg.159]    [Pg.116]    [Pg.9]    [Pg.594]    [Pg.1171]    [Pg.1263]    [Pg.936]    [Pg.120]    [Pg.71]    [Pg.76]    [Pg.178]    [Pg.65]    [Pg.483]    [Pg.165]    [Pg.771]    [Pg.347]    [Pg.372]    [Pg.23]    [Pg.257]    [Pg.175]    [Pg.291]    [Pg.225]    [Pg.681]    [Pg.386]    [Pg.288]    [Pg.226]    [Pg.97]    [Pg.152]    [Pg.122]   
See also in sourсe #XX -- [ Pg.332 ]




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